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用于评估抗非复制型结核分枝杆菌药物效力的生物发光法。

Bioluminescence for assessing drug potency against nonreplicating Mycobacterium tuberculosis.

作者信息

Vocat Anthony, Hartkoorn Ruben C, Lechartier Benoit, Zhang Ming, Dhar Neeraj, Cole Stewart T, Sala Claudia

机构信息

Global Health Institute, Ecole Polytechnique Fédérale de Lausanne, Lausanne, Switzerland.

Global Health Institute, Ecole Polytechnique Fédérale de Lausanne, Lausanne, Switzerland

出版信息

Antimicrob Agents Chemother. 2015 Jul;59(7):4012-9. doi: 10.1128/AAC.00528-15. Epub 2015 Apr 20.

Abstract

Targeting dormant Mycobacterium tuberculosis represents a challenge to antituberculosis drug discovery programs. We previously reported and validated the use of the streptomycin (STR)-dependent M. tuberculosis 18b strain as a tool for assessing drug potency against nonreplicating bacteria both in vitro and in vivo. In this study, we generated a luminescent 18b strain, named 18b-Lux, by transforming the bacteria with a vector expressing the luxCDABE operon from Photorhabdus luminescens. Luciferase expression was demonstrated under replicating conditions, and, more importantly, luminescence levels significantly above background were detected following STR removal. The sensitivity of STR-starved 18b-Lux to approved and candidate antituberculosis therapeutic agents was evaluated by means of a luciferase assay in a 96-well format. Results mirrored the data obtained with the standard resazurin reduction microplate assay, and the luminescence readout allowed time course assessments of drug efficacy in vitro. Specifically, we proved that bedaquiline, the rifamycins, and sutezolid displayed time-dependent activity against dormant bacteria, while pyrazinamide and SQ109 showed bactericidal effects at the highest concentrations tested. Overall, we established the optimal conditions for an inexpensive, simple, and very sensitive assay with great potential for future applications.

摘要

靶向潜伏性结核分枝杆菌是抗结核药物研发项目面临的一项挑战。我们之前报道并验证了使用依赖链霉素(STR)的结核分枝杆菌18b菌株作为在体外和体内评估药物对非复制型细菌效力的工具。在本研究中,我们通过用表达来自发光杆菌属的luxCDABE操纵子的载体转化细菌,构建了一种发光的18b菌株,命名为18b-Lux。在复制条件下证实了荧光素酶的表达,更重要的是,在去除STR后检测到发光水平显著高于背景。通过96孔板的荧光素酶测定法评估了STR饥饿的18b-Lux对已批准和候选抗结核治疗药物的敏感性。结果与通过标准刃天青还原微孔板测定法获得的数据一致,并且发光读数允许在体外对药物疗效进行时间进程评估。具体而言,我们证明了贝达喹啉、利福霉素和舒他西林对休眠细菌具有时间依赖性活性,而吡嗪酰胺和SQ109在测试的最高浓度下显示出杀菌作用。总体而言,我们建立了一种廉价、简单且非常灵敏的测定法的最佳条件,具有很大的未来应用潜力。

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本文引用的文献

1
Simple and rapid method to determine antimycobacterial potency of compounds by using autoluminescent Mycobacterium tuberculosis.
Antimicrob Agents Chemother. 2014 Oct;58(10):5801-8. doi: 10.1128/AAC.03205-14. Epub 2014 Jul 21.
2
In vitro and in vivo activities of three oxazolidinones against nonreplicating Mycobacterium tuberculosis.
Antimicrob Agents Chemother. 2014 Jun;58(6):3217-23. doi: 10.1128/AAC.02410-14. Epub 2014 Mar 24.
3
Multitarget drug discovery for tuberculosis and other infectious diseases.
J Med Chem. 2014 Apr 10;57(7):3126-39. doi: 10.1021/jm500131s. Epub 2014 Apr 1.
4
para-Aminosalicylic acid is a prodrug targeting dihydrofolate reductase in Mycobacterium tuberculosis.
J Biol Chem. 2013 Aug 9;288(32):23447-56. doi: 10.1074/jbc.M113.475798. Epub 2013 Jun 18.
5
Rapid in vivo assessment of drug efficacy against Mycobacterium tuberculosis using an improved firefly luciferase.
J Antimicrob Chemother. 2013 Sep;68(9):2118-27. doi: 10.1093/jac/dkt155. Epub 2013 Apr 30.
6
CD271(+) bone marrow mesenchymal stem cells may provide a niche for dormant Mycobacterium tuberculosis.
Sci Transl Med. 2013 Jan 30;5(170):170ra13. doi: 10.1126/scitranslmed.3004912.
7
Para-aminosalicylic acid acts as an alternative substrate of folate metabolism in Mycobacterium tuberculosis.
Science. 2013 Jan 4;339(6115):88-91. doi: 10.1126/science.1228980. Epub 2012 Nov 1.
8
Streptomycin-starved Mycobacterium tuberculosis 18b, a drug discovery tool for latent tuberculosis.
Antimicrob Agents Chemother. 2012 Nov;56(11):5782-9. doi: 10.1128/AAC.01125-12. Epub 2012 Aug 27.
9
Inhibition of mycolic acid transport across the Mycobacterium tuberculosis plasma membrane.
Nat Chem Biol. 2012 Feb 19;8(4):334-41. doi: 10.1038/nchembio.794.
10
Autoluminescent Mycobacterium tuberculosis for rapid, real-time, non-invasive assessment of drug and vaccine efficacy.
PLoS One. 2012;7(1):e29774. doi: 10.1371/journal.pone.0029774. Epub 2012 Jan 11.

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